F20 Radiopaque Bone Cement - Indonesia BPOM Medical Device Registration
F20 Radiopaque Bone Cement is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302024941. The device is manufactured by TEKNIMED SAS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TEKNIMED SASCountry of Origin
France
Authorized Representative
PT. FAJAR SELARAS PARTNERSAR Address
Komplek Rukan PTC Blok 8C No. 28-29 Pulogadung Tel. 021-46827776 Fax. 021-46827033
Registration Date
Aug 31, 2020
Expiry Date
Feb 14, 2025
Product Type
Prosthetic Orthopedic Equipment
Polymethylmethacrylate (PMMA) bone cement.
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